The Knight Prostate Cancer Research Program is seeking a Therapeutic Interventional (TI) Sr. Clinical Research Assistant (Clinical Research Coordinator) working on complex therapeutic interventional (TI) clinical research protocols and data management.
This TI Sr. Clinical Research Assistant position will be part of the Knight Clinical Research Prostate Program and is responsible for implementation and overall management of oncology clinical trials.
These responsibilities include coordination of all aspects of a study as specifically outlined in the protocol. Primary focus will be subject safety and compliance with the prescribed protocol and Good Clinical Practice. The CRC will work collaboratively with physician, nursing, and ancillary staff in the scheduling and management of subject research activities. The CRC will maintain accurate, complete and timely records on all research subjects including preparation of source documentation and clinical research data/case report forms. . The CRC will have direct patient contact, process biological samples and perform other non invasive testing such as ECGs and vitals.
Given the complexities of oncology research and the challenges of working with a terminally ill population, strong customer service, organizational, and interpersonal skills are required. Ability to clearly organize and/or adapt to multiple priorities and deadlines at one time is necessary. Attention to detail, service orientation, delegation and project management skills, and above average critical judgment skills are essential.
Key Responsibilities:
Education & experience:
Knowledge, skills, and abilities:
Education & experience:
Knowledge, skills, and abilities:
Apply online. Please be sure to upload a Cover Letter and Resume/CV.
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